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Associate Ii, Complex Gx, Regulatory Affairs

Teva Pharmaceuticals
Teva Pharmaceuticals
4+ years
preferred by company
10 Dec. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate II – Complex Generics, Regulatory Affairs (US FDA)

Company: Teva Pharmaceuticals
Location: Bangalore, India
Employment Type: Full-Time
Function: Regulatory Affairs – Complex Generics
Industry: Pharmaceuticals / Generic & Specialty Medicines
Experience Required: 4+ Years
Job ID: 63167
Posting Date: December 11, 2025


About Teva Pharmaceuticals

Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating across nearly 60 countries with a diverse and inclusive workforce. As one of the world’s largest manufacturers of generic medicines and a key contributor to the World Health Organization’s Essential Medicines List, Teva helps more than 200 million patients worldwide access high-quality, affordable healthcare every day.


Role Overview

The Associate II – Complex Generics, Regulatory Affairs is responsible for preparing and submitting high-quality US FDA regulatory filings for complex generic products, including inhalation, ophthalmic, implantable, and drug–device combination products. This role supports both pre-approval and post-approval regulatory activities and requires close collaboration with cross-functional stakeholders to ensure compliance, quality, and on-time submissions.

Working with moderate to minimal supervision, the Associate II manages original applications, amendments, deficiency responses, and post-approval supplements while supporting regulatory strategy execution and process improvement initiatives.


Key Responsibilities

  • Prepare, review, and compile US FDA regulatory submissions using a right-first-time approach, including:

    • Original applications

    • Amendments

    • Deficiency responses (IRs, DRLs, CRLs)

  • Support early FDA engagement strategies to align development plans and reduce regulatory risk

  • Evaluate regulatory impact of change controls, including site transfers, formulation changes, and alternate API sourcing

  • Determine appropriate post-approval submission pathways (PAS, CBE-30, CBE-0, Annual Reports) in alignment with FDA and internal SOPs

  • Compile and submit post-approval supplements ensuring compliance with FDA, ICH, and internal regulatory requirements

  • Serve, as needed, as a regulatory point of contact for cross-functional teams such as R&D, QA, Manufacturing, Packaging, and DMF holders

  • Monitor and manage regulatory timelines, proactively identifying and resolving data or documentation gaps

  • Track and interpret updates to FDA regulations and guidance documents relevant to complex generics

  • Monitor FDA databases (e.g., Drugs@FDA, Orange Book) and communicate relevant regulatory changes internally

  • Participate in audits, inspections, and continuous process improvement initiatives


Required Experience & Qualifications

  • Master’s degree in Regulatory Affairs or Quality Assurance, preferably in Pharmaceuticals

  • Minimum 4+ years of pharmaceutical industry experience, with exposure to:

    • Inhalation products

    • Ophthalmic products

    • Implants

    • Drug–device combination products

  • Prior experience in Regulatory Affairs, Analytical, QA, laboratory, or manufacturing environments preferred

  • Strong understanding of ICH guidelines and US FDA regulatory requirements

  • Excellent written and verbal communication skills

  • Strong organizational abilities with attention to detail and effective multitasking skills

  • Demonstrated critical thinking, problem-solving, and regulatory judgment


Why Join Teva

  • Work on high-impact, complex generic products regulated by the US FDA

  • Gain exposure to advanced regulatory pathways and drug–device combination technologies

  • Collaborate with global, cross-functional teams

  • Opportunity for long-term career growth in a globally recognized pharmaceutical organization

  • Inclusive and performance-driven work culture


Equal Employment Opportunity Statement

Teva Pharmaceuticals is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, religion, gender, disability, pregnancy, sexual orientation, gender identity or expression, national origin, or any other legally protected status. Reasonable accommodations are available throughout the recruitment process upon request.


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